ClearanceBrief
510(k) K896835 ยท LKB Pad, Alcohol, Device Disinfectant

ALCOHOL PREP AND POVIDONE-IODINE PREP

ApplicantNorpak Mfg., Inc., Ajax, Ontario L1z 1e2, CA
DecisionSubstantially Equivalent, Jan 11, 1990
ReceivedDec 5, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K896835

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.